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CANNON II PLUS CHRONIC HEMODIALYSIS CATHETER, EDGE CHRONIC HEMODIALYSIS CATHETER, NEXTSTEP(R) RETROGRADE CHRONIC...

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111117
510(k) Type
Special
Applicant
Teleflex Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
6/30/2011
Days to Decision
70 days
Submission Type
Summary

CANNON II PLUS CHRONIC HEMODIALYSIS CATHETER, EDGE CHRONIC HEMODIALYSIS CATHETER, NEXTSTEP(R) RETROGRADE CHRONIC...

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111117
510(k) Type
Special
Applicant
Teleflex Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
6/30/2011
Days to Decision
70 days
Submission Type
Summary